Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session

36P - EP300 as an epigenetic target in p53 wild-type tumors treated with cisplatin

Date

15 Oct 2022

Session

Poster display session

Presenters

Agnieszka Robaszkiewicz

Citation

Annals of Oncology (2022) 33 (suppl_8): S1383-S1430. 10.1016/annonc/annonc1095

Authors

A. Robaszkiewicz, K. Gronkowska

Author affiliations

  • University of Lodz, Department of General Biophysics, Lodz/PL

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 36P

Background

Cisplatin is used as first-line chemotherapy treatment for patients diagnosed with various types of malignancies, such as leukemia, lymphomas, breast, testicular, ovarian, head and neck, non-small lung, cervical cancers, and sarcomas. However, our recent study provided evince on the activation of DNA repair genes in p53 wild-type of breast, non-small lung and liver cancer, but not in mutated triple-negative breast cancer or p53 deficient myeloid leukemia.

Methods

RNA- and ChIP-Seq, cellular technics (toxicity, confocal immunostaining, western blot, real-time PCR) we found p53 wild-type interaction with EP300 at the promoters of PARP1, BRCA1 and RAD51.

Results

RNA-Seq data confirmed that pharmacological inhibition of ATM/ATR, EP300 and transient silencing of p53 prevent overexpression of genes contributing to nucleotide excision repair (GO:0006289), double-strand break repair via homologous recombination (GO:0000724) and nonhomologous end joining (GO:0006303) and DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest (GO:0006977). This was not observed in p53 single-nucleotide or deletion mutants. Since transcription of majority of genes involved in DNA repair is controlled by cell cycle progression via E2F activity, we paid attention to p53 interaction with chromatin upon cisplatin treatment. ChIP-Seq data confirmed the enrichment of approximately 1200 genomic locations, where only 7% overlapped with E2F1, but 22% with EP300 peaks. Prediction of target genes linked p53 enriched regions with genes assigned to nucleotide-excision repair and DNA damage recognition (GO:0000715). Cisplatin caused p53 co-localization with EP300 in the nuclei, but E2F1 silencing restrained the enrichment of both proteins on chromatin. Pharmacological inhibition of ATR/ATM, EP300 and p53 silencing considerably increased cisplatin cytotoxicity. The same effect of EP300 inhibitors on cisplatin cytotoxicity was observed in cisplatin-resistant p53 wild-type breast and non-small lung cancers.

Conclusions

ATM/ATR-p53/E2F1/EP300 pathway allows cells to increase resistance to cisplatin. Addition of EP300 inhibitors may improve cisplatin-based chemotherapies of p53 wild-type cancers and improve chemotherapy outcome.

Legal entity responsible for the study

The authors.

Funding

National Center for Research and Development (LIDER/22/0122/L-10/18/NCBR/2019) and Ministry of Education and Science (IDUB-60/2021).

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.